Bleed-to-Read on the BioQule Library Preparation system for NGS. A complete, walk-away solution to turn blood samples into ready-to-sequence NGS libraries.

The accessibility of Next-Generation Sequencing (NGS) is increasing, but there is still a bottleneck in the NGS process when it comes to nucleic acid (NA) purification and preparing sequencing-ready libraries. The main challenge lies in the absence of a reliable and user-friendly automation system specifically designed for low throughput NA purification and library preparation. To address this issue, Revvity has developed the BioQule™ NGS System, which offers a comprehensive solution that fully automates both NA purification from just 30 – 40 µL of whole blood and library preparation for up to 8 samples in a walk-away workflow. This system minimizes human error and minimizes hands-on time to just 20 minutes. The BioQule™ NGS System is an ideal solution for automating library preparation from human whole blood (BLEED from a finger prick), providing a fully walk-away sample preparation and quantification (READ to sequencing) in a small, benchtop solution.
For research use only. Not for use in diagnostic procedures.